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Local and systemic antibody response in infants after oral administration of inactivated enteropathogenic E. coli

R Lodinová-Zádníková1, B Korych, K Gajdostíková

  • 1Institute for Care of Mother and Child, Prague.

Folia Microbiologica
|January 1, 1990
PubMed

Insights

Infants under one month produced IgM and IgA antibodies in the gut after an E. coli vaccine. Older infants (2-7 months) primarily showed IgA responses in the gut, with serum antibody levels unchanged in both groups.

Area of Science:

  • Immunology
  • Pediatrics
  • Microbiology

Background:

  • Enteropathogenic Escherichia coli (E. coli) strains O111 and O55 are significant causes of infant gastroenteritis.
  • Understanding the infant immune response to oral vaccines is crucial for developing effective prevention strategies.

Purpose of the Study:

  • To investigate the dynamics and formation of antibody isotypes in the intestine and serum of infants following oral administration of inactivated enteropathogenic E. coli strains.
  • To compare the immune responses in two infant age groups: up to one month and 2-7 months old.

Main Methods:

  • Ten infants were divided into two age groups (up to 1 month and 2-7 months).
  • Infants received oral inactivated E. coli strains O111 and O55 (first and booster doses).
  • Antibody isotypes (IgM, IgA, IgG) in stool and serum were analyzed using indirect immunofluorescence over 30 days.

Main Results:

  • Infants up to one month old produced IgM and IgA antibodies in stool after both vaccine doses.
  • Serum IgG antibodies increased within 2-5 days after each dose in younger infants.
  • Infants aged 2-7 months predominantly showed an IgA response in stool after vaccination.
  • Serum immunoglobulin levels remained unchanged in the older infant group post-vaccination.

Conclusions:

  • Age significantly influences the type and location of antibody responses to oral E. coli vaccination in infants.
  • Younger infants mount a mixed IgM/IgA response locally, with transient systemic IgG increase.
  • Older infants exhibit a more mature IgA-dominant mucosal response without significant systemic changes.

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